"Ambry Genetics"[submitter] AND "PGR"[gene] - ClinVar

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Items: 49

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2351123	NM_000926.4(PGR):c.2780C>A (p.Pro927His)	PGR (P333H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2290442	NM_000926.4(PGR):c.2323A>G (p.Met775Val)	PGR (M509V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3306040	NM_000926.4(PGR):c.2076G>A (p.Met692Ile)	PGR (M528I +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3306035	NM_000926.4(PGR):c.1982G>A (p.Gly661Asp)	PGR (G497D +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2247482	NM_000926.4(PGR):c.1783A>G (p.Met595Val)	PGR (M1V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3211900	NM_000926.4(PGR):c.1678G>A (p.Glu560Lys)	PGR (E396K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3306038	NM_000926.4(PGR):c.1670A>G (p.Tyr557Cys)	PGR (Y393C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3211899	NM_000926.4(PGR):c.1628A>G (p.Asn543Ser)	PGR (N379S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2243348	NM_000926.4(PGR):c.1615C>T (p.Pro539Ser)	PGR (P375S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2460067	NM_000926.4(PGR):c.1475G>T (p.Arg492Leu)	PGR (R328L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2287293	NM_000926.4(PGR):c.1472C>G (p.Pro491Arg)	PGR (P327R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3211897	NM_000926.4(PGR):c.1444G>A (p.Ala482Thr)	PGR (A318T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2243948	NM_000926.4(PGR):c.1438T>G (p.Cys480Gly)	PGR (C316G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2346975	NM_000926.4(PGR):c.1343T>C (p.Val448Ala)	PGR (V448A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2204881	NM_000926.4(PGR):c.1301C>G (p.Pro434Arg)	PGR (P434R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2352287	NM_000926.4(PGR):c.1271C>G (p.Pro424Arg)	PGR (P260R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2554644	NM_000926.4(PGR):c.1244C>G (p.Pro415Arg)	PGR (P251R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2234865	NM_000926.4(PGR):c.1231C>G (p.Pro411Ala)	PGR (P247A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3306034	NM_000926.4(PGR):c.1223G>A (p.Gly408Asp)	PGR (G244D +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3306039	NM_000926.4(PGR):c.1184A>G (p.Glu395Gly)	PGR (E395G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2221470	NM_000926.4(PGR):c.1184A>C (p.Glu395Ala)	PGR (E231A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3211895	NM_000926.4(PGR):c.1135G>A (p.Asp379Asn)	PGR (D215N +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2456079	NM_000926.4(PGR):c.1120T>G (p.Tyr374Asp)	PGR (Y210D +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3211894	NM_000926.4(PGR):c.1012G>A (p.Ala338Thr)	PGR (A174T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2612567	NM_000926.4(PGR):c.976G>A (p.Asp326Asn)	PGR (D326N +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3306037	NM_000926.4(PGR):c.896C>A (p.Thr299Lys)	PGR (T135K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3211907	NM_000926.4(PGR):c.863C>G (p.Pro288Arg)	PGR (P124R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3211906	NM_000926.4(PGR):c.841G>T (p.Ala281Ser)	PGR (A281S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2493823	NM_000926.4(PGR):c.830C>G (p.Ala277Gly)	PGR (A113G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2350210	NM_000926.4(PGR):c.809A>G (p.Lys270Arg)	PGR (K106R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2318897	NM_000926.4(PGR):c.782C>G (p.Ala261Gly)	PGR (A261G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2237229	NM_000926.4(PGR):c.760G>C (p.Ala254Pro)	PGR (A254P +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3306036	NM_000926.4(PGR):c.704C>T (p.Pro235Leu)	PGR (P235L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2286739	NM_000926.4(PGR):c.691G>A (p.Glu231Lys)	PGR (E67K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3306041	NM_000926.4(PGR):c.671A>T (p.Glu224Val)	PGR (E224V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3211904	NM_000926.4(PGR):c.662T>A (p.Val221Asp)	PGR (V57D +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2607642	NM_000926.4(PGR):c.640C>G (p.Pro214Ala)	PGR (P214A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3211903	NM_000926.4(PGR):c.562G>A (p.Gly188Ser)	PGR (G188S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2250192	NM_000926.4(PGR):c.490C>A (p.Leu164Ile)	PGR (L164I)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3211902	NM_000926.4(PGR):c.442C>T (p.Pro148Ser)	PGR (P148S)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2386612	NM_000926.4(PGR):c.413G>A (p.Ser138Asn)	PGR (S138N)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2362978	NM_000926.4(PGR):c.385C>T (p.Pro129Ser)	PGR (P129S)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3306033	NM_000926.4(PGR):c.370C>T (p.Pro124Ser)	PGR (P124S)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2274542	NM_000926.4(PGR):c.332T>C (p.Leu111Pro)	PGR (L111P)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3211901	NM_000926.4(PGR):c.259T>A (p.Tyr87Asn)	PGR (Y87N)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3211898	NM_000926.4(PGR):c.149C>A (p.Ala50Asp)	PGR (A50D)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2292821	NM_000926.4(PGR):c.122C>T (p.Thr41Ile)	PGR (T41I)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2613017	NM_000926.4(PGR):c.85T>C (p.Cys29Arg)	PGR (C29R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2221137	NM_000926.4(PGR):c.29G>A (p.Arg10Gln)	PGR (R10Q)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance

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Items: 49